Name: Biomedical Engineering Courses
Price: 100 GBP
Availability: InStock

<div id="course-pills-1">Duration<p>3 Days</p><p>18 CPD hours</p>This course is intended for<p>CliniciansUniversitiesHospitalsHealthcare ExecutivesEntrepreneursInvestors</p>Overview<p>Intro to blockchainMajor healthcare use cases of blockchainUnderstand different use cases of PEB that have already been implemented and encourage thought of new potential use cases.</p><p>This course covers the intersection of healthcare and Blockchain.   Training will include an overview of Blockchain, and uses for Blockchain in the healthcare industry, from medical records, to medical devices, insurance and more.</p></div><div id="course-pills-2"><h4>Day 1</h4><ul><li>History of blockchain</li><li>Blockchain 101</li><li>Decentralization/centralization</li><li>Distributed ledger-private vs public</li><li>Mining and consensus mechanisms</li><li>Intro to healthcare on blockchain including Medical records FHIR, HL7</li></ul><h4>Day 2</h4><ul><li>Patient identity</li><li>Value-based care and concepts (discuss outcome-based smart contracts)</li><li>Medical devices, Wearables, IoT </li><li>Patient adherence monitoring (with tokenized incentives-could also discuss with pt. empowerment), incentives, etc.</li><li>Interoperability and other obstacles of implementation (industry inertia, large data sets, inherent resistance to change)</li></ul><h4>Day 3</h4><ul><li>Supply chain (substandard and falsified medicines, divergence, compliance with DSCSA)</li><li>Logistics</li><li>Insurance (eligibility, reduced overhead, claims processing)</li><li>Data sets</li><li>AI technology (theoretical use cases)</li><li>PT empowerment 1 &amp; 2 (digital health wallet with access driven by smart contracts, monetizing data for sharing)</li></ul></div><div id="course-pills-3"><h4>Additional course details:</h4><br /><p>Nexus Humans Blockchain for Healthcare Professionals training program is a workshop that presents an invigorating mix of sessions, lessons, and masterclasses meticulously crafted to propel your learning expedition forward. </p><p></p> This immersive bootcamp-style experience boasts interactive lectures, hands-on labs, and collaborative hackathons, all strategically designed to fortify fundamental concepts. <p></p>Guided by seasoned coaches, each session offers priceless insights and practical skills crucial for honing your expertise. Whether you're stepping into the realm of professional skills or a seasoned professional, this comprehensive course ensures you're equipped with the knowledge and prowess necessary for success.  <p></p>While we feel this is the best course for the Blockchain for Healthcare Professionals course and one of our Top 10 we encourage you to read the course outline to make sure it is the right content for you.  <p></p>Additionally, private sessions, closed classes or dedicated events are available both live online and at our training centres in Dublin and London, as well as at your offices anywhere in the UK, Ireland or across EMEA.<p></p></div>

Nexus Human

Healthcare IT

Cryptocurrency & Blockchain

Health Coach Training

Trainers Course

Healthcare Marketing

Healthcare

Blockchain for Healthcare Professionals

<p>Quality assurance (QA) is the systematic process of determining whether or not items match customer expectations. Our quality assurance training can help you prevent issues when providing solutions or services to customers.</p><p>QA develops and maintains strict specifications for designing, manufacturing, and providing services. A quality assurance system aims to improve work practises and productivity. It can also be used to boost customer confidence, enhance a company's reputation, and position the company to compete with or exceed its competitors. Our training helps participants improve their problem-solving, analytical, and interpersonal skills. Anyone working in manufacturing, production, pharmaceutical, biopharma, medical technology, or medical devices may find this course helpful. After finishing the course, participants will have a solid understanding of the duties of quality technician, quality supervisor, and quality coordinator.</p><p><strong>Learning outcome of this QA - Quality Assurance Course:</strong></p><ul><li>Learn how to create, implement, and sustain error-free performance to provide further value to customers.</li><li>To revolutionise any business operation, the ability to continuously develop workable quality systems is required.</li><li>Capability to apply key quality assurance and quality control methodologies, techniques, and concepts to improve the quality culture of any organisation.</li><li>You will be able to conduct an effective root cause analysis to identify areas for improvement and implement your findings.</li><li>Will be able to apply quality strategies to improve decision-making skills.</li></ul><p><strong>Why People Enrol this QA - Quality Assurance Manager at QLS Level 3 from One Education:</strong></p><ul><li>Receive a Quality Licence Scheme-endorsed certificate upon successful completion of the</li><li>Learning materials of our course contains engaging voiceover and visual elements for your comfort</li><li>Get 24/7 access to all course content for a full year</li><li>Complete the course at your own pace</li><li>Each of our students gets full tutor support on weekdays (Monday to Friday)</li><li>Efficient assessments and instant results upon completion of our course</li></ul><p>This online training course is designed by industry experts and will give you an in-depth understanding of this topic. The QA - Quality Assurance Manager at QLS Level 3 course features easy-to-digest modules that break down each topic and ensure all our students receive an unrivalled and thorough learning experience.</p><p>If you want to work in this rapidly growing sector and stand out from the competition, then our QA - Quality Assurance Manager at QLS Level 3 course is the perfect place to kickstart your dream career.</p><p><strong>Course Curriculum:</strong></p><p>Here is a curriculum breakdown of the course:</p><ul><li>Concept of Quality</li><li>Customer Input to Quality</li><li>Plan Quality</li><li>Quality Control</li><li>Six Sigma</li></ul><p><strong>How is the course assessed?</strong></p><p>To simplify the procedure of evaluation and accreditation for learners, we provide an automated assessment system. Upon completion of an online module, you will immediately be given access to a specifically crafted MCQ test. The results will be evaluated instantly, and the score displayed for your perusal. For each test, the pass mark will be set to 60%.</p><p>When all tests have been successfully passed, you will be able to claim a certificate endorsed by the Quality Licence Scheme.</p><p><strong>Certificate of Achievement</strong></p><p><strong>Endorsed Certificate of Achievement from the Quality Licence Scheme</strong></p><p>After successfully completing the course, learners will get an endorsed certificate (included with the course) delivered right at their doorstep by post, without paying a single penny! Please note that learners residing outside the UK have to pay a £10 postage charge.</p><p><strong>CPD Accredited Certification from One Education</strong></p><p>After successfully completing the MCQ assessment of this course, you will also qualify for a CPD Accredited Certificate from One Education, as proof of your continued professional development. Certification is available in PDF format, at the cost of £9, or a hard copy can be sent to you via post, at the cost of £15.</p><h2>
        
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    </h2>

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                                        10 CPD hours / points
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                                            Accredited by CPD Quality Standards
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                                </div>
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        <div>Who is this course for?</div>
    </h2>

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                            <p>This course is designed for</p><ul><li>Engineers, manufacturing and production managers/personnel</li><li>Operations managers and personnel</li><li>General managers and chief operating officers</li><li>Business owners and leaders</li><li>Corporate executives</li><li>Quality assurance coordinators, supervisors and managers</li><li>Quality control coordinators, supervisors and managers</li></ul><p><br /><br /></p>
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        <div>Requirements</div>
    </h2>

                        <div id="requirements">
                            <p>There are no formal entry requirements for the course, with enrollment open to anyone!<strong> Anyone and everyone</strong> with a knack for learning can enrol on this course without any hesitation.</p><p>Learn online from any internet device, including your computer, tablet or smartphone. Study when it suits you and complete the course at your own pace.</p><p>All students must have a passion for learning and literacy, as well as being over the age of 16.</p>
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        <div>Career path</div>
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                        <div id="career_path">
                            <p>Understanding QA - Quality Assurance will provide you with a competitive advantage and open the door to a variety of professional prospects. One can develop into:</p><ul><li>Quality assurance manager (Salary: £23,000 to £55,000)</li><li>Quality control assistant (Salary: £20,000 to £30,000)</li><li>Food manufacturing inspector (Salary: £20,000 to £35,000)</li><li>Ofsted inspector (Salary: £46,362 to £75,500)</li></ul><p><br /><br /></p>
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        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>QLS Endorsed Certificate</h4>
        <p>
            Hard copy certificate -
            Included
        </p>

                        </div>

One Education

QA - Quality Assurance Manager at QLS Level 3 Course

General Admission

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					<p><span>This comprehensive course on </span><b><span>European Medical Device Regulations</span></b> will deepen your understanding on this topic.</p><p><span><span>After successful completion of this course you can acquire the required skills in this sector. This </span><b>European Medical Device Regulations</b> comes with accredited certification, which will enhance your CV and make you worthy in the job market.</span></p><p><span><span>So enrol in this course today to fast track your career ladder.</span></span></p>					</div>
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			<h2>How will I get my certificate?</h2>		</div>
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					<p>You may have to take a quiz or a written test online during or after the course. After successfully completing the course, you will be eligible for the certificate.</p>					</div>
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			<h2>Who is This course for?</h2>		</div>
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					<p><span>There is no experience or previous qualifications required for enrolment on this </span><b><span>European Medical Device Regulations</span></b>. It is available to all students, of all academic backgrounds.</p>					</div>
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					<p><span>Our </span><b><span>European Medical Device Regulations</span></b> is fully compatible with PC's, Mac's, Laptop, Tablet and Smartphone devices. This course has been designed to be fully compatible with tablets and smartphones so you can access your course on Wi-Fi, 3G or 4G.</p><p><span><span>There is no time limit for completing this course, it can be studied in your own time at your own pace.</span></span></p>					</div>
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					<p><span>Having these various qualifications will increase the value in your CV and open you up to multiple sectors such as Business &amp; Management, Admin, Accountancy &amp; Finance, Secretarial &amp; PA, Teaching &amp; Mentoring etc.</span></p>					</div>
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					</div> <h3>Course Curriculum</h3><div><p>1 sections • 4 lectures • 02:26:00 total length</p></div><div><div><div><div><div><div><div><p>•Module 1: Overview to European Regulations on Medical Devices: 00:43:00</p></div><div><div><p>•Module 2: Essential Components of EU MDR: 00:40:00</p></div><div><div><p>•Module 3: Reporting Requirements and Identification: 00:27:00</p></div><div><div><p>•Module 4: Quality System in Medical Device Regulation: 00:36:00</p></div></div></div></div></div></div></div></div></div></div>

Apex Learning

Certificate in Further Education & Training (Cert Ed)

Certificate in Emergency Response Ambulance Driving (CERAD)

Medical Training

European Computer Driving Licence (ECDL)

Medical Education

European Medical Device Regulations

<strong>Want to learn about Kubernetes security or need to pass the Certified Kubernetes Security Specialist (CKS) exam? You are at the right place. A hands-on course to help you develop your Kubernetes security skills. You need to have a basic understanding of Kubernetes Administrator to get the best out of this course.</strong>
        <p>This Kubernetes Security Specialist course provides foundational knowledge using concepts and hands-on demonstrations of the Kubernetes Cluster.

In this course, we will be focusing more on the practical side, so make sure you have a running Kubernetes cluster. This course is focused on security. It deals with all aspects of security within the context of a Kubernetes environment. That means securing not only the Kubernetes cluster itself but also the applications running within the cluster.

You will learn how to secure many different components of Kubernetes applications and environments. We are going to cover every topic such as cluster setup, creating an ingress, and securing an ingress. You will also learn cluster hardening, which includes RBAC, role, and role binding for a user.

Further, you will learn system hardening, kernel hardening, minimizing microservice vulnerabilities, supply chain security, monitoring, logging, and runtime security.

By the end of this Kubernetes course, you will gain in-depth knowledge about Kubernetes and be a Kubernetes security specialist.

All resources and code files are placed here: https://github.com/PacktPublishing/A-Certified-Kubernetes-Security-Specialist-CKS-Course</p>
        <h2>What You Will Learn</h2><p>Learn how to create a Kubernetes Cluster<br>Learn how to create default deny NetworkPolicy<br>Learn how to install Kubernetes Dashboard<br>Learn how to download and verify Kubernetes release<br>Explore role and role binding for a user<br>Learn how to create a Kubernetes cluster with the outdated version</p>
        <h2>Audience</h2><p>This Docker course is designed for Kubernetes administrators, security specialists, and for those who want to master Certified Kubernetes Security Specialist.<br><br>You should already have some Kubernetes Administrator knowledge before attending this course.</p>
        <h2>Approach</h2><p>This Docker course is very hands-on; it provides you with not only the theory but also real-life examples of developing Docker applications that you can try out on your own laptop.</p>
        <h2>Key Features</h2><p>Deep technical insight into Kubernetes * Learn to use kubesec to perform static analysis using Docker image * Learn how to use Falco to find malicious processes</p>
        <h2>Github Repo</h2><p>https://github.com/PacktPublishing/A-Certified-Kubernetes-Security-Specialist-CKS-Course</p>
        <h2>About the Author</h2><h3>Himanshu Sharma</h3><p>Himanshu Sharma is an expert in Kubernetes, containers, and cloud-native infrastructure. He has more than 12 years of IT experience in a variety of industries, including medical devices, entertainment, enterprise software, and cloud computing. He is passionate about learning new technologies and believes the best way to learn is by doing it practically.</p>
        <h2>Course Outline</h2><h4>1. You Can Become a Certified Kubernetes Security Specialist (CKS)</h4><p></p><br><h4>2. Create Kubernetes Cluster</h4><p></p><br><h4>3. Cluster Setup - Use Network security policies to restrict cluster level access</h4><p></p><br><h4>4. Cluster Setup - Minimize use of, and access to, GUI elements</h4><p></p><br><h4>5. Cluster Setup - Properly set up Ingress objects with security control</h4><p></p><br><h4>6. Protect node metadata and endpoints</h4><p></p><br><h4>7. Use CIS benchmark to review the security configuration of Kubernetes components</h4><p></p><br><h4>8. Verify platform binaries before deploying</h4><p></p><br><h4>9. Cluster Hardening - RBAC (Role Based Access Control)</h4><p></p><br><h4>10. Exercise caution in using service accounts</h4><p></p><br><h4>11. Cluster Hardening - Restrict API Access</h4><p></p><br><h4>12. Cluster Hardening - Upgrade Kubernetes</h4><p></p><br><h4>13. Microservice Vulnerabilities - Manage Kubernetes Secrets</h4><p></p><br><h4>14. Use container runtime sandboxes in multi-tenant env (e.g. gvisor,kata container)</h4><p></p><br><h4>15. Microservice Vulnerabilities - OS Level Security Domains</h4><p></p><br><h4>16. Microservice Vulnerabilities - mTLS</h4><p></p><br><h4>17. Open Policy Agent (OPA)</h4><p></p><br><h4>18. Supply Chain Security - Image Footprint</h4><p></p><br><h4>19. Supply Chain Security - Static Analysis</h4><p></p><br><h4>20. Supply Chain Security - Image Vulnerability Scanning</h4><p></p><br><h4>21. Supply Chain Security - Secure Supply chain</h4><p></p><br><h4>22. Behavioral Analytics at host and container level</h4><p></p><br><h4>23. Runtime Security - Immutability of containers at runtime</h4><p></p><br><h4>24. Runtime Security - Auditing</h4><p></p><br><h4>25. System Hardening - Kernel Hardening</h4><p></p>

Packt

CKAD

Kubernetes

Want to learn about Kubernetes security or need to pass the Certified Kubernetes Security Specialist (CKS) exam? You are at the right place. A hands-on course to help you develop your Kubernetes security skills. You need to have a basic understanding of Kubernetes Administrator to get the best out of this course.

Certified Kubernetes Security Specialist (CKS) Course

<p>Embark on a journey into the world of Medical Gases Safety and Handling with our comprehensive course. Delve into the critical modules, beginning with an insightful Introduction to Medical Gases. Move on to mastering Safety and Handling Guidelines, crucial for ensuring the well-being of patients and healthcare professionals alike. Explore the nuances of Common Medical Gases, gaining in-depth knowledge of their applications and precautions.</p><p>Next, delve into Storage, Transportation, and Documentation, vital aspects of maintaining a seamless supply chain in healthcare settings. Understand the intricacies of Administration Techniques and Monitoring, honing skills that are indispensable in any medical environment. Finally, cap off your learning with Practical Skills and Simulation, putting theory into practice through hands-on experience.</p><p><strong>Key Features</strong></p><ul><li>CPD Accredited</li><li>FREE PDF + Hardcopy certificate</li><li>Fully online, interactive course</li><li>Self-paced learning and laptop, tablet and smartphone-friendly</li><li>24/7 Learning Assistance</li><li>Discounts on bulk purchases</li></ul><p><strong>Course Curriculum of Medical Gases<br /></strong></p><ul><li>Module 01 : Introduction to Medical Gases</li><li>Module 02 : Safety and Handling Guidelines</li><li>Module 03 : Common Medical Gases</li><li>Module 04 : Storage, Transportation, and Documentation</li><li>Module 05 : Administration Techniques and Monitoring</li><li>Module 06 : Practical Skills and Simulation</li></ul><p>Learning Outcomes:</p><ul><li>Acquire a comprehensive understanding of Medical Gases and their applications.</li><li>Implement Safety and Handling Guidelines effectively in healthcare settings.</li><li>Identify and differentiate between Common Medical Gases, ensuring accurate usage.</li><li>Demonstrate proficiency in Storage, Transportation, and Documentation of medical gases.</li><li>Master Administration Techniques and Monitoring for optimal patient care.</li><li>Apply Practical Skills through realistic simulations, enhancing confidence and competence.</li></ul><p><strong>Accreditation</strong></p><p>This course is <strong>CPD Quality Standards</strong> (<strong>CPD QS)</strong> accredited, providing you with up-to-date skills and knowledge and helping you to become more competent and effective in your chosen field.</p><h2>
        
        <div>CPD</div>
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                        <div id="cpd">
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                                        10 CPD hours / points
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                                            Accredited by CPD Quality Standards
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        <div>Who is this course for?</div>
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                        <div id="who_is_this_course_for">
                            <ul><li>Healthcare professionals seeking to bolster their knowledge of medical gases.</li><li>Nursing staff and caregivers involved in the administration of medical gases.</li><li>Emergency responders and technicians dealing with medical gas-related situations.</li><li>Health and safety officers responsible for compliance in medical facilities.</li><li>Biomedical engineers and technicians involved in medical gas systems.</li><li>Students pursuing healthcare-related courses seeking specialized knowledge.</li><li>Regulatory and quality assurance professionals in the healthcare sector.</li><li>Individuals looking to expand their skill set for career advancement.</li></ul>
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        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <ul><li>Medical Gas Technician</li><li>Healthcare Compliance Officer</li><li>Biomedical Equipment Technician</li><li>Clinical Educator (Medical Gases)</li><li>Health and Safety Coordinator (Healthcare)</li><li>Regulatory Affairs Specialist (Medical Devices)</li></ul>
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        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>Digital certificate</h4>
        <p>
            Digital certificate -
            Included
        </p>
            <div><p>Once you've successfully completed your course, you will immediately be sent a FREE digital certificate.</p></div>
        <h4>Hard copy certificate</h4>
        <p>
            Hard copy certificate -
            Included
        </p>
            <div><p>Also, you can have your FREE printed certificate delivered by post (shipping cost £3.99 in the UK).<br />For all international addresses outside of the United Kingdom, the delivery fee for a hardcopy certificate will be only <strong>£10</strong>.<br />Our certifications have no expiry dates, although we do recommend that you renew them every 12 months.</p></div>

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Training Express

Medical Gases Safety and Handling Guidelines Course

<p>Are you aware that improper disposal of sharps poses serious risks, including the transmission of bloodborne diseases such as <strong>Hepatitis B, C, and HIV</strong>? Whether you work in a healthcare setting or simply handle medical devices at home or work, understanding the risks and responsibilities associated with sharps is crucial.</p><p><strong>Course Highlights:</strong></p><ul><li>Explore the Different Types of Sharp Medical Equipment<br /></li><li>Understand Vital Health and Safety Regulations Concerning Sharps<br /></li><li>Learn Safe Handling Procedures to Minimise Risks<br /></li><li>Discover Proven Methods for Accident Prevention with Sharps<br /></li><li>Understand Roles and Responsibilities When Using Sharps<br /></li><li>Gain Knowledge on Responsible Sharps Disposal</li></ul><p><strong>Key Features: </strong></p><ul><li>Accredited by CPD Quality Standards</li><li>Instant FREE e-certificate</li><li>Fully online, interactive with audio voiceover</li><li>Self-paced learning and laptop, tablet, smartphone-friendly</li><li>24/7 Learning Assistance</li><li>Discounts on bulk purchases</li></ul><p><strong>Learning Outcomes:</strong></p><p>Upon completing the course, you will be equipped to:</p><ul><li>Safely handle various sharp medical equipment.</li><li>Comply with essential health and safety regulations.</li><li>Minimise risks associated with sharps through proper procedures.</li><li>Prevent accidents and injuries related to sharps use.</li><li>Fulfill roles and responsibilities when dealing with sharps.</li><li>Dispose of sharps in a responsible and secure manner.</li></ul><p><strong>Course Curriculum</strong></p><p>The detailed curriculum outline of our Sharps Training Course is as follows:</p><ul><li><strong>Module 01:</strong> Introduction to Sharps</li><li><strong>Module 02:</strong> Regulations Concerning Sharps</li><li><strong>Module 03:</strong> Safe Handling Procedures</li><li><strong>Module 04:</strong> Reducing the Associated Risks</li><li><strong>Module 05:</strong> Duties and Responsibilities of Personnel</li><li><strong>Module 06:</strong> Safe Disposal of Sharps</li></ul><p>Enroll in our Sharps Training Course today to enhance your safety knowledge, comply with regulations, and contribute to a secure and responsible healthcare environment. Don't miss this opportunity to stay ahead in your career!</p><p><strong>Accreditation</strong></p><p>All of our courses included in this Sharps Training course is fully CPD QS accredited, providing you with up-to-date skills and knowledge and helping you to become more competent and effective in your chosen field.</p><p><strong>Certification</strong></p><p>Once you've successfully completed your course, you will immediately be sent digital certificates for the bundle courses.</p><h2>
        
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                                        10 CPD hours / points
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                                            Accredited by CPD Quality Standards
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        <div>Who is this course for?</div>
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                            <p>Anyone with a knack for learning new skills can take this course, including:</p><ul><li>Nurses working in hospitals, clinics, or care facilities.</li><li>Phlebotomists responsible for drawing blood samples from patients.</li><li>Health care workers involved in patient care and treatment.</li><li>Caregivers providing assistance to individuals in home care settings.</li><li>Anyone seeking to enhance their knowledge of sharps safety protocols.</li></ul>
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        <div>Requirements</div>
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                            <p>There are no formal requirements for this course to be enrolled.</p>
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        <div>Career path</div>
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                            <ul><li>Nursing</li><li>Phlebotomy</li><li>Healthcare Assistant</li><li>Care Support Worker</li><li>Occupational Health Nursing</li><li>Clinical Nursing and Child Care</li><li>First Aider</li></ul>
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        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>PDF Certificate</h4>
        <p>
            Digital certificate -
            Included
        </p>

                        </div>

Sharps Training for Nurse, Phlebotomist, Health Care Workers, & Caregivers Course

<div fr-original-style="" style="box-sizing: border-box;"><h2 fr-original-style="" style="box-sizing: border-box;"> About Course</h2><div fr-original-style="" style="box-sizing: border-box;"><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><strong fr-original-style="" style="font-weight: 700; box-sizing: border-box;">The human body is a masterpiece of engineering and a work of art. Biomedical Engineers form the vanguard of new approaches to understand disease progression rationally and develop new diagnostic and therapeutic strategies to keep humans safe and healthy.</strong></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;">Biomedical engineering is a rapidly growing field that offers exciting opportunities for students and professionals alike. Biomedical engineers are involved in the development of new and innovative medical devices, systems, and therapies. They also play a vital role in the research and development of new drugs and treatments.</p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;">This course will provide you with the fundamental engineering principles and knowledge that are essential for a successful career in biomedical engineering. You will learn about the different types of biomedical engineering, including bioinstrumentation, biosignal processing, biomedical imaging systems, and biomechanics. You will also have the opportunity to gain hands-on experience with biomedical devices and systems.</p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><strong fr-original-style="" style="font-weight: 700; box-sizing: border-box;">Why You Should Take This Course</strong></p><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;">Learn the fundamental engineering principles and knowledge that are essential for a successful career in biomedical engineering.</li><li fr-original-style="" style="box-sizing: border-box;">Gain hands-on experience with biomedical devices and systems.</li><li fr-original-style="" style="box-sizing: border-box;">Prepare for a variety of careers in biomedical engineering, such as research, development, design, manufacturing, and sales.</li><li fr-original-style="" style="box-sizing: border-box;">Gain the skills and knowledge necessary to develop and commercialize new biomedical products and technologies.</li><li fr-original-style="" style="box-sizing: border-box;">Learn how to apply engineering principles to solve real-world biomedical problems.</li><li fr-original-style="" style="box-sizing: border-box;">Have the opportunity to collaborate with other students and faculty on cutting-edge research projects.</li><li fr-original-style="" style="box-sizing: border-box;">Develop the critical thinking and problem-solving skills that are essential for success in any field.</li></ul><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><strong fr-original-style="" style="font-weight: 700; box-sizing: border-box;">Enroll today and start your journey to becoming a biomedical engineer!</strong></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><strong fr-original-style="" style="font-weight: 700; box-sizing: border-box;">Become a part of the vanguard of new approaches to understand disease progression rationally and develop new diagnostic and therapeutic strategies to keep humans safe and healthy.</strong></p></div></div> <div fr-original-style="" style="box-sizing: border-box;"><h3 fr-original-style="" style="box-sizing: border-box;"> What Will You Learn?</h3><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Define biomedical engineering and explain its importance in the field of healthcare.</span></li><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Identify the different types of biomedical engineers and their roles.</span></li><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Apply engineering principles to solve real-world biomedical problems.</span></li><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Apply biomechanics principles to the study of the human body and the design of medical devices and implants.</span></li><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Communicate effectively with other biomedical engineers, healthcare professionals, and the public about biomedical engineering research and advancements.</span></li></ul></div><div fr-original-style="" style="box-sizing: border-box;"><h3 fr-original-style="" style="box-sizing: border-box;"> Course Content</h3><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><h4 fr-original-style="" style="box-sizing: border-box;"> Introduction to Biomedical Engineering</h4><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span><h5 fr-original-style="" style="box-sizing: border-box;"> Introduction to Biomedical Engineering</h5></div><div fr-original-style="" style="box-sizing: border-box;"> </div></li></ul></div></div></div><div fr-original-style="" style="box-sizing: border-box;"><h4 fr-original-style="" style="box-sizing: border-box;"> Introduction to Physiology</h4><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span><h5 fr-original-style="" style="box-sizing: border-box;"> Introduction to Physiology</h5></div><div fr-original-style="" style="box-sizing: border-box;"> </div></li></ul></div></div></div><div fr-original-style="" style="box-sizing: border-box;"><h4 fr-original-style="" style="box-sizing: border-box;"> Bioinstrumentation</h4><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span><h5 fr-original-style="" style="box-sizing: border-box;"> Bioinstrumentation</h5></div><div fr-original-style="" style="box-sizing: border-box;"> </div></li></ul></div></div></div><div fr-original-style="" style="box-sizing: border-box;"><h4 fr-original-style="" style="box-sizing: border-box;"> Biosignal Processing</h4><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span><h5 fr-original-style="" style="box-sizing: border-box;"> Biosignal Processing</h5></div><div fr-original-style="" style="box-sizing: border-box;"> </div></li></ul></div></div></div><div fr-original-style="" style="box-sizing: border-box;"><h4 fr-original-style="" style="box-sizing: border-box;"> Biomedical Imaging Systems</h4><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span><h5 fr-original-style="" style="box-sizing: border-box;"> Biomedical Imaging Systems</h5></div><div fr-original-style="" style="box-sizing: border-box;"> </div></li></ul></div></div></div><div fr-original-style="" style="box-sizing: border-box;"><h4 fr-original-style="" style="box-sizing: border-box;"> Biomechanics</h4><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span><h5 fr-original-style="" style="box-sizing: border-box;"> Biomechanics</h5></div><div fr-original-style="" style="box-sizing: border-box;"> </div></li></ul></div></div></div></div></div>A course by  Xpert Learning  RequirementsBasic understanding of Biology Audience  Students in the fields of engineering, science, and medicine  Healthcare professionals<h3 fr-original-style="" style="box-sizing: border-box;"> Audience</h3><ul fr-original-style="" style="box-sizing: border-box;"><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Students in the fields of engineering, science, and medicine</span></li><li fr-original-style="" style="box-sizing: border-box;"> <span fr-original-style="" style="box-sizing: border-box;"></span> <span fr-original-style="" style="box-sizing: border-box;">Healthcare professionals</span></li></ul>

Xpert Learning

Biomedical Science

Biomechanics

Biomedical Engineer

Biomedical Engineering

Biomedicine

Biomedical

Introduction to  Biomedical Engineering

<section>
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			<h2>Overview</h2>		</div>
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							<p><span>By enroling in Essentials of European Medical Device Regulations, you can kickstart your vibrant career and strengthen your profound knowledge. You can learn everything you need to know about the topic.</span></p><p><span>The Essentials of European Medical Device Regulations course includes all of the most recent information to keep you abreast of the employment market and prepare you for your future. The curriculum for this excellent Essentials of European Medical Device Regulations course includes modules at all skill levels, from beginner to expert. You will have the productivity necessary to succeed in your organisation once you have completed our Essentials of European Medical Device Regulations Program.</span></p><p><span>So enrol in our Essentials of European Medical Device Regulations course right away if you're keen to envision yourself in a rewarding career.</span></p>						</div>
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			<h2><b>Description</b>
</h2>		</div>
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							<p><span>Enroling in this Essentials of European Medical Device Regulations course can improve your Essentials of European Medical Device Regulations perspective, regardless of your skill levels in the Essentials of European Medical Device Regulations topics you want to master. If you're already a Essentials of European Medical Device Regulations expert, this peek under the hood will provide you with suggestions for accelerating your learning, including advanced Essentials of European Medical Device Regulations insights that will help you make the most of your time. This Essentials of European Medical Device Regulations course will act as a guide for you if you've ever wished to excel at Essentials of European Medical Device Regulations.</span></p>						</div>
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			<h2>Why Choose Us?</h2>		</div>
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							<ul><li><span>After successfully completing the Essentials of European Medical Device Regulations Course, you will receive a </span><b>FREE PDF Certificate </b><span>as evidence of your newly acquired abilities.</span></li><li><span>Lifetime access to the whole collection of Essentials of European Medical Device Regulations learning materials.</span></li><li><span>Online test with immediate results</span></li><li><span>Enroling in the course has no additional cost.</span></li><li><span>You can study and complete the Essentials of European Medical Device Regulations course at your own pace.</span></li><li><span>Study for the Essentials of European Medical Device Regulations course using any internet-connected device, such as a computer, tablet, or mobile device.</span></li></ul>						</div>
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			<h2>Who Is This Course For?</h2>		</div>
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							<p><span>This Essentials of European Medical Device Regulations course is a great place to start if you're looking to start a new career in Essentials of European Medical Device Regulations field. This training is for anyone interested in gaining in-demand Essentials of European Medical Device Regulations proficiency to help launch a career or their business aptitude. </span></p>						</div>
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			<h2>Requirements</h2>		</div>
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							<p><span>The Essentials of European Medical Device Regulations course requires no prior degree or experience. All you require is English proficiency, numeracy literacy and a gadget with stable internet connection. Learn and train for a prosperous career in the thriving and fast-growing industry of Essentials of European Medical Device Regulations, without any fuss.</span></p>						</div>
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			<h2>Career Path</h2>		</div>
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							<p><span>This Essentials of European Medical Device Regulations training will assist you develop your Essentials of European Medical Device Regulations ability, establish a personal brand, and present a portfolio of relevant talents. It will help you articulate a  Essentials of European Medical Device Regulations professional story and personalise your path to a new career. Furthermore, developing this Essentials of European Medical Device Regulations skillset can lead to numerous opportunities for high-paying jobs in a variety of fields.</span></p>						</div>
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				<h3>
	<span>Course Curriculum</span>
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					<td colspan="4">Essentials of European Medical Device Regulations</td>
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					<td><i></i></td>
					<td>Module 1: Overview to European Regulations on Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:43:00</span></td>
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					<td><i></i></td>
					<td>Module 2: Essential Components of EU MDR</td>
					<td> </td>
					<td><span><i></i> 00:40:00</span></td>
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					<td><i></i></td>
					<td>Module 3: Reporting Requirements and Identification</td>
					<td> </td>
					<td><span><i></i> 00:27:00</span></td>
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					<td><i></i></td>
					<td>Module 4: Quality System in Medical Device Regulation</td>
					<td> </td>
					<td><span><i></i> 00:36:00</span></td>
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					<td colspan="4">Assignment</td>
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					<td><i></i></td>
					<td>Assignment - Essentials of European Medical Device Regulations</td>
					<td> </td>
					<td><span><i></i> 00:00:00</span></td>
				</tr>
				</tbody></table></div>

			</div>

NextGen Learning

Essentials of European Medical Device Regulations Course

<div>
	<h3><b>Description:</b></h3>
<p><span>Want to pursue your career in medication management? Or are you currently working as a nurse, midwives, clinical supporters, or home domiciliary care workers? Then Medication Management for Nurses and Midwives course is the best choice for you.</span></p>
<p><span>Proper Medication management allows the patients optimal therapeutic outcomes from the prescription medications. Therefore, proper knowledge of medication management is a must for the people who are in responsible for giving medications to the patients. </span></p>
<p><span>The course familiarizes you with the concepts of medication including along with the process of storage and dispensing, administration of medication and more.  You will know about the legislation involved with the administration of medication. The course trains you how to minimize, reduce or eliminates medication errors. </span></p>
<p><span>Shortly, you will gain a solid understanding of medication management.</span></p>
<h3><b>Assessment:</b></h3>
<p>This course does not involve any MCQ test. Students need to answer assignment questions to complete the course, the answers will be in the form of written work in pdf or word. Students can write the answers in their own time. Once the answers are submitted, the instructor will check and assess the work.</p>
<h3><strong>Certification:</strong></h3>
<p>After completing and passing the course successfully, you will be able to obtain an Accredited Certificate of Achievement. Certificates can be obtained either in hard copy at a cost of £39 or in PDF format at a cost of £24.</p>
<h3><b>Who is this Course for?</b></h3>
<p><b>Medication Management for Nurses and Midwives </b>is certified by CPD Qualifications Standards and CiQ. This makes it perfect for anyone trying to learn potential professional skills.</p>
<p>As there is no experience and qualification required for this course, it is available for all students from any academic background.</p>
<h3><b>Requirements</b></h3>
<p>Our<b> Medication Management for Nurses and Midwives</b> is fully compatible with any kind of device. Whether you are using Windows computer, Mac, smartphones or tablets, you will get the same experience while learning. Besides that, you will be able to access the course with any kind of internet connection from anywhere at any time without any kind of limitation.</p>
<h3><b>Career Path</b></h3>
<p>After completing this course you will be able to build up accurate knowledge and skills with proper confidence to enrich yourself and brighten up your career in the relevant job market.</p>
		</div><table width="100%">				<tbody><tr>
					<td colspan="4">General Principles and Responsibilities</td>
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					<td><i></i></td>
					<td>Legislation</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
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					<td><i></i></td>
					<td>Key Principles</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
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					<td><i></i></td>
					<td>Five Rights of Medication Administration</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
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					<td><i></i></td>
					<td>Double-checking Medications</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
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					<td><i></i></td>
					<td>Monitoring and documentation of medication management</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
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					<td>Patient/service-user Education</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
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					<td>Considerations for Withholding of Medication</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
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					<td colspan="4">The Cycle of Medication Management</td>
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					<td><i></i></td>
					<td>Transcription of Prescription/Medication Order</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Use of Facsimile</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Medication Administration</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Dispensing of Medicinal Products</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Scheduled MDA Drugs</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Management of MDA Schedule 2 Drugs</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Storage of Medicinal Products</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Safety in Medication Management</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Medication Errors</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Crushing Medications</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Immunisations and vaccinations</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Adverse Drug Reaction</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Incidents Involving Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Medication Protocols</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Medication Protocols</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Medication Protocol Framework Template</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Appendices</td>
					<td> </td>
					<td><span><i></i> 00:30:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Terms Relating to Medication Management</td>
					<td> </td>
					<td><span><i></i> 00:30:00</span></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>References - Medication Management</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Assessment</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Assignment - Medication Management for Nurses and Midwives</td>
					<td> </td>
					<td><span><i></i> 00:00:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Order Your Certificate and Transcript</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Order Your Certificates and Transcripts</td>
					<td> </td>
					<td><span><i></i> 00:00:00</span></td>
				</tr>
				</tbody></table>

John Academy

GNM (General Nursing & Midwifery)

Medication

Medication Administration

NHS Management

Nursing & Midwifery

Medicine Management

Medication Management for Nurses and Midwives

<p>Tired of browsing and searching for the course you are looking for? Can't find the complete package that fulfils all your needs? Then don't worry as you have just found the solution. Take a minute and look through this 14-in-1 extensive bundle that has everything you need to succeed in Biomedical Engineering and other relevant fields!</p><p>After surveying thousands of learners just like you and considering their valuable feedback, this all in one Biomedical Engineering bundle has been designed by industry experts. We prioritised what learners were looking for in a complete package and developed this in-demand Biomedical Engineering course that will enhance your skills and prepare you for the competitive job market.</p><p>Also, our Biomedical Engineering experts are available for answering your queries and help you along your learning journey. Advanced audiovisual learning modules of these courses are broken down into little chunks so that you can learn at your own pace without being overwhelmed by too much material at once.</p><p>Furthermore, to help you showcase your expertise in Biomedical Engineering, we have prepared a special gift of 1 hardcopy certificate and 1 PDF certificate for the title course completely free of cost. These certificates will enhance your credibility and encourage possible employers to pick you over the rest.</p><p><strong>This Biomedical Engineering Bundle Consists of the following Premium courses: </strong></p><ul><li><strong>Course 01: </strong>European Medical Device Regulations</li><li><strong>Course 02: </strong>Public Health</li><li><strong>Course 03: </strong>Human Anatomy and Physiology</li><li><strong>Course 04: </strong>Epidemiology</li><li><strong>Course 05: </strong>Biomedical Science</li><li><strong>Course 06: </strong>Diploma In Microbiology</li><li><strong>Course 07: </strong>Biotechnology</li><li><strong>Course 08: </strong>Microbiology Technician Course</li><li><strong>Course 09: </strong>Digital Electric Circuits &amp; Intelligent Electrical Devices</li><li><strong>Course 10: </strong>COSHH Awareness Level 3</li><li><strong>Course 11: </strong>Electrical and Fire Safety Training - Level 2</li><li><strong>Course 12: </strong>Emergency First Aid and Incident Management at Work</li><li><strong>Course 13: </strong>Creativity and Problem Solving Skills</li><li><strong>Course 14: </strong>Pandemic Disease Awareness</li></ul><p><strong>Benefits you'll get choosing Apex Learning:</strong></p><ul><li>Pay once and get lifetime access to 14 CPD courses</li><li>Certificates, student ID for the title course included in a one-time fee</li><li>Free up your time - don't waste time and money travelling for classes</li><li>Accessible, informative modules designed by expert instructors</li><li>Learn at your ease - anytime, from anywhere</li><li>Study the course from your computer, tablet or mobile device</li><li>CPD accredited course - improve the chance of gaining professional skills</li></ul><p><strong>How will I get my Certificate?</strong></p><p>After successfully completing the course, you will be able to order your CPD Accredited Certificates (PDF + Hard Copy) as proof of your achievement.</p><ul><li><strong>PDF Certificate: Free (For The Title Course)</strong></li><li><strong>Hard Copy Certificate: Free (For The Title Course)</strong></li></ul><p>Curriculum of <strong>Bundle </strong></p><p><strong>Course 01: European Medical Device Regulations</strong></p><ul><li>Overview to European Regulations on Medical Devices</li><li>Essential Components of EU MDR</li><li>Reporting Requirements and Identification</li><li>Quality System in Medical Device Regulation</li></ul><p><strong>Course 02: Public Health</strong></p><ul><li>Introduction to Public Health</li><li>Principles of Public Health</li><li>Understanding Epidemiology</li><li>Disease Control</li><li>Understanding Measures of Disease Frequency</li><li>Maternity and Childbirth</li><li>Environment and Public Health</li><li>Health System and Policy</li><li>Public Health and Ethics</li></ul><p><strong>Course 03: Human Anatomy and Physiology</strong></p><ul><li>Human Body Vocabulary with Pictures</li><li>Equipment, Instruments and Lab Tests</li><li>Acronyms and Abbreviation</li><li>Digestive System</li><li>Cardiovascular System</li><li>Blood and Immunity System</li><li>Respiratory System</li><li>Musculoskeletal System</li><li>Central Nervous System</li></ul><p><strong>Course 04: Epidemiology</strong></p><ul><li>Understanding Epidemiology</li><li>Principles of Epidemiology</li><li>Study Design</li><li>Disease Occurrence</li><li>Variation in Disease by Time, Place, and Person</li><li>Epidemics and Outbreaks</li><li>Measures of Risk and Disease Prevention</li><li>Measures of Disease Frequency</li><li>Role of Epidemiology in Public Health</li><li>The Epidemiological Concept of Population</li></ul><p><strong>Course 05: Biomedical Science</strong></p><ul><li>Introduction to Biomedical Science</li><li>Genetics and Biochemistry</li><li>Microbiology and Cell Biology</li><li>Biochemical Engineering and Enzyme Discovery</li><li>Toxicology, Pharmaceuticals and Fine Chemicals</li><li>Systems and Synthetic Biology</li><li>Global Health Challenges</li></ul><p><strong>Course 06: Diploma In Microbiology</strong></p><ul><li>Introduction to Microbiology</li><li>Cell Structure and Organisation</li><li>The Chemical Metabolism</li><li>Microbial Growth Controlling</li><li>Microbial Diversity Prokaryote Diversity</li><li>Microbial Diversity Eukaryote Diversity</li><li>Viruses, Viroids, and Prions</li><li>Interactions between Microbes and Humans</li><li>Human Microbial Diseases</li><li>Immunity</li><li>Vaccines and Antimicrobial Agents</li><li>Microorganisms in the Environment</li><li>Industrial and Food Microbiology</li></ul><p><strong>Course 07: Biotechnology</strong></p><ul><li>Introduction to Biotechnology</li><li>Biotechnology in the Realm of History</li><li>Molecular and Cellular Biology</li><li>Biotechnology Versus Molecular Biology</li><li>Genetic Engineering</li><li>Biotechnology in Health Sector</li><li>Industrial Biotechnology</li><li>Biotechnology in a Business Perspective</li></ul><p><strong>Course 08: Microbiology Technician Course</strong></p><ul><li>Introduction to Microbiology</li><li>Cell Structure and Organisation</li><li>Microbial Diversity Prokaryote Diversity</li><li>Microbial Diversity Eukaryote Diversity</li><li>Viruses, Viroids, and Prions</li><li>Interactions between Microbes and Humans</li><li>Human Microbial Diseases</li><li>Microorganisms in the Environment</li><li>Laboratory Equipments (Part-01)</li><li>Laboratory Equipments (Part-02)</li><li>Solutions Used in Clinical/Medical Laboratory</li><li>Sterilisation, Disinfection and Decontamination</li><li>Laboratory Accidents and Safety</li></ul><p><strong>Course 09: Digital Electric Circuits &amp; Intelligent Electrical Devices</strong></p><ul><li>Introduction</li><li>Numbering Systems</li><li>Binary Arithmetic</li><li>Logic Gates</li><li>Flip-Flops</li><li>Counters &amp; Shift Registers</li><li>Adders</li></ul><p><strong>Course 10: COSHH Awareness Level 3</strong></p><ul><li>COSHH Explained</li><li>COSHH Regulations</li><li>Health Problems Related to Hazardous Substances</li><li>Identifying Hazardous Substances</li><li>COSHH Risk Assessments</li><li>Control Measures and Monitoring</li><li>Implementing Control Measures</li></ul><p><strong>Course 11: Electrical and Fire Safety Training - Level 2</strong></p><ul><li>Introduction and Basics</li><li>Introduction to Fire Safety</li><li>Voltage and Resistance</li><li>Capacitance and Capacitors</li><li>Safety Precautions</li><li>Fire Safety Legislation</li><li>Measures of Fire Safety</li><li>Fire Emergency: Evacuation Procedures</li></ul><p><strong>Course 12: Emergency First Aid and Incident Management at Work</strong></p><ul><li>Introduction to Workplace First Aid</li><li>Legal Framework for Workplace First Aid</li><li>Incident Management at Work</li><li>Primary Survey</li><li>Secondary Survey</li><li>Basic First-Aid Techniques</li><li>Dealing with Minor Injuries at the Workplace</li><li>Secondary Illness Loss of Responsiveness and CPR</li><li>Secondary Illness Breathing Problems</li><li>Secondary Illnesses and Injuries</li><li>Dealing With Fractures and Dislocations</li><li>Call for an Emergency</li></ul><p><strong>Course 13: Creativity and Problem Solving Skills</strong></p><ul><li>Getting Started</li><li>The Problem Solving Method</li><li>Information Gathering</li><li>Problem Definition</li><li>Preparing for Brainstorming</li><li>Generating Solutions (I)</li><li>Generating Solutions (II)</li><li>Analyzing Solutions</li><li>Selecting a Solution</li><li>Planning Your Next Steps</li><li>Recording Lessons Learned</li></ul><p><strong>Course 14: Pandemic Disease Awareness</strong></p><ul><li>Introduction to Pandemics</li><li>Pandemics: Risks, Impacts, and Mitigation</li><li>The SARS - MERS Factors</li><li>The Novel Coronavirus (2019-nCoV) 2020 Version of the SARS</li><li>Zoonotic Diseases</li><li>Pandemic Outbreaks from History (HIV/Aids), (Influenza), (Nipah Virus), (Smallpox), (Viral Meningitis), (Ebola Virus), (Zika Virus), (Plague)</li><li>Mild Threats to Human-Being</li><li>Pandemic Risks and Consequences</li><li>Pandemic Mitigation: Preparedness And Response</li></ul><h2>
        
        <div>CPD</div>
    </h2>

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                                        140 CPD hours / points
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                                            Accredited by CPD Quality Standards
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        <div>Who is this course for?</div>
    </h2>

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                            <p>Anyone from any background can enrol in this Biomedical Engineering bundle.</p><p>** Completing this course does not imply that you are qualified to work as a Biomedical Scientist. If you are seeking a course that fits the HCPC's standards, please contact the HCPC or the RCSLT **</p>
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        <div>Requirements</div>
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                            <p>Our Biomedical Engineering course is fully compatible with PCs, Macs, laptops, tablets and Smartphone devices.</p>
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        <div>Career path</div>
    </h2>

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                            <p>Having this Biomedical Engineering expertise will increase the value of your CV and open you up to multiple job sectors.</p>
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        <div>Certificates</div>
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                                    <h4>Certificate of completion</h4>
        <p>
            Digital certificate -
            Included
        </p>
            <div> <p>You will get the PDF Certificate for the title course (<strong>European Medical Device Regulations</strong>) absolutely Free! </p> </div>
        <h4>Certificate of completion</h4>
        <p>
            Hard copy certificate -
            Included
        </p>
            <div> <p>You will get the Hard Copy certificate for the title course (<strong>European Medical Device Regulations</strong>) absolutely Free! Other Hard Copy certificates are available for £10 each. </p><p>Please Note: The delivery charge inside the UK is £3.99, and the international students must pay a £9.99 shipping cost.</p> </div>

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Biomedical Engineering Courses

<p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" id="isPasted" fr-original-style=" color: rgb(51, 51, 51);">This module provides an introduction to the basics of medical device regulation, especially the requirements that manufacturers must meet in order to market devices in Europe and the USA.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">We explain what medical devices are and give examples of the various types. We outline the principles of their regulation and the criteria for placing them on the market. We identify major players in regulation worldwide.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">We then outline prominent characteristics of the regulation of medical devices in the USA and in Europe. The module is up to date with the current upheaval in European Union legislation on medical devices.</p>

Zenosis

Good Manufacturing Practice (GMP)

Biotechnology

Pharmaceutical

Pharmacology

Drug Safety

Medical

This module provides an introduction to the basics of medical device regulation, especially the requirements that manufacturers must meet in order to market devices in Europe and the USA.

MD01: An Introduction to the Regulation of Medical Devices

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                            <p> </p>
<p>During this training course, you will also gain a thorough understanding of the best practices of Medical Devices Quality Management Systems and be able to improve an organization`s overall performance by consistently providing safe and qualitative medical devices.</p>
<p>After mastering all the necessary concepts of Medical Devices Quality Management Systems, you can sit for the exam and gain the "Certified ISO 13485 Lead Implementer' Certificate. By holding this Certificate, you will be able to demonstrate that you have the practical knowledge and professional capabilities to implement ISO 13485 in an organization. </p>
                        </div>
                    </div>
                    <div>
                        <h2>About This Course</h2>
                        <div>
                            <p> </p>
<p>Learning Objectives</p>
<ul>
<li>Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks </li>
<li>Master the concepts, approaches, methods and techniques used for the implementation and effective management of a MDQMS</li>
<li>Learn how to interpret the ISO 13485 requirements in the specific context of an organization</li>
<li>Learn how to support an organization to effectively plan, implement, manage, monitor and maintain a MDQMS</li>
<li>Acquire the expertise to advise an organization in implementing Medical Devices Quality Management System best practices</li>
</ul>
<p> </p>
<p>Course Agenda</p>
<ul>
<li><span><strong>Day 1</strong>:</span> Introduction to ISO 13485 and initiation of a MDQMS</li>
<li><span><strong>Day 2</strong>:</span> Plan the implementation of a MDQMS</li>
<li><span><strong>Day 3</strong>:</span> Implementation of a MDQMS</li>
<li><strong>Day 4:</strong> MDQMS monitoring, measurement, continuous improvement and preparation for a certification audit, and the final exam.</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Assessment</h2>
                        <div>
                            <p> </p>
<p> </p>
<p>Delegates sit a combined exam, consisting of in-course quizzes and exercises, as well as a final 12 question, essay type exam on Day 4 of the course. The overall passing score is 70%, to be achieved within the 150 minute time allowance.</p>
<p>Exam results are provided within 24 hours, with both a Certificate and a digital badge provided as proof of success.</p>
                        </div>
                    </div>
                    <div>
                        <h2>Prerequisites</h2>
                        <div>
                            <p> </p>
<p><span>A fundamental understanding of ISO 13485 and comprehensive knowledge of implementation principles.</span></p>
                        </div>
                    </div>
                    <div>
                        <h2>What's Included?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Certification fees are included on the exam price</li>
<li>Training material containing over 450 pages of information and practical examples will be distributed</li>
<li>An attestation of course completion worth 32 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.</li>
<li>In case of exam failure, you can retake the exam within 12 months for free</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Who Should Attend?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Managers or consultants involved in Medical Devices Quality Management</li>
<li>Expert advisors seeking to master the implementation of a Medical Devices Quality Management System</li>
<li>Individuals responsible for maintaining conformance with MDQMS requirements</li>
<li>MDQMS team members</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Accreditation</h2>
                        <div>
                            <p><img src="https://www.the-training-centre.com/content/img/National%20Accreditation%20Service%20(3).jpg" height="201" width="258" /></p>
                        </div>
                    </div>
                    <div>
                        <h2>Provided by</h2>
                        <div>
                            <p> </p>
<p>This course is Accredited by <a title="NACS" href="http://www.nacs.ee" target="_blank">NACS</a> and Administered by the <a title="IECB" href="https://www.iecb.org" target="_blank">IECB</a></p>
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Training Centre

ISO 13485 Lead Implementer

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                            <p> </p>
<p><span>ISO 13485 Foundation training enables you to learn the basic elements to implement and manage a Medical Devices Quality Management System (MDQMS) as specified in ISO 13485. During this training course, you will be able to understand the different modules of a MDQMS, including MDQMS policy, procedures, performance measurements, management commitment, internal audit, management review and continual improvement.</span></p>
<p><span><span>After completing this course, you can sit for the exam and gain "Certified ISO 13485 Foundation' Certification. This Certificate shows that you have understood the fundamental methodologies, requirements, framework and management approach. </span></span></p>
                        </div>
                    </div>
                    <div>
                        <h2>About This Course</h2>
                        <div>
                            <p> </p>
<p>Learning Objectives</p>
<ul>
<li>Understand the elements and operations of a Medical Devices Quality Management System (MDQMS)</li>
<li>Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks</li>
<li>Understand the approaches, methods and techniques used for the implementation and  management of a MDQMS</li>
</ul>
<p> </p>
<p>Course Agenda</p>
<ul>
<li>
<p><span>Day 1</span>: Introduction to Medical Devices Quality Management System (MDQMS) concepts as required by ISO 13485</p>
</li>
<li>
<p>Day 2: Medical Devices Quality Management System requirements and Certification Exam  </p>
</li>
</ul>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Assessment</h2>
                        <div>
                            <p> </p>
<p> </p>
<p>Delegates sit a combined exam, consisting of in-course quizzes and exercises, as well as a final 40 question, multiple choice exam on Day 2 of the course. The overall passing score is 70%, to be achieved within the 60 minute time allowance.</p>
<p>Exam results are provided within 24 hours, with both a Certificate and a digital badge provided as proof of success.</p>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Prerequisites</h2>
                        <div>
                            <p> </p>
<p><span>None</span></p>
                        </div>
                    </div>
                    <div>
                        <h2>What's Included?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Certification fees are included on the exam price</li>
<li>Training material containing over 200 pages of information and practical examples will be distributed</li>
<li>An attestation of course completion worth 14 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Who Should Attend?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Individuals involved in Medical Devices Quality Management</li>
<li>Individuals seeking to gain knowledge about the main processes of Medical Devices Quality Management Systems (MDQMS)</li>
<li>Individuals interested to pursue a career in Medical Devices Quality Management</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Accreditation</h2>
                        <div>
                            <p><img src="https://www.the-training-centre.com/content/img/National%20Accreditation%20Service%20(3).jpg" height="201" width="258" /></p>
                        </div>
                    </div>
                    <div>
                        <h2>Provided by</h2>
                        <div>
                            <p> </p>
<p>This course is Accredited by <a title="NACS" href="http://www.nacs.ee" target="_blank">NACS</a> and Administered by the <a title="IECB" href="https://www.iecb.org" target="_blank">IECB</a></p>
                        </div>
                    </div>

ISO 13485 Quality Management Foundation

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                        <div>
                            <p> </p>
<p>During this training course, delegates will acquire the knowledge and skills to plan and carry out internal and external audits in compliance with ISO 19011 and ISO/IEC 17021-1 certification process.</p>
<p>Based on practical exercises, you will learn audit techniques and become competent to manage an audit program, audit team, communication with customers, and understand reporting requirements.</p>
<p>After acquiring the necessary expertise to perform this audit, you can sit for the exam and gain the "Certified ISO 13485 Lead Auditor' Certificate. By holding this Certificate, delegates can demonstrate that they have the competencies to audit organizations based on best practices.</p>
                        </div>
                    </div>
                    <div>
                        <h2>About This Course</h2>
                        <div>
                            <p> </p>
<p><strong>Learning Outcomes</strong></p>
<p> </p>
<ul>
<li>Review a Medical Devices Quality Management System based on ISO 13485</li>
<li>Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks</li>
<li>Understand an auditor's role to: plan, lead and follow-up on a management system audit in accordance with ISO 19011</li>
<li>Learn how to lead an audit and audit team</li>
<li>Learn how to interpret the requirements of ISO 13485 in the context of a MDQMS audit</li>
<li>Acquire the competencies of an auditor to: plan an audit, lead an audit, draft reports, and follow-up on an audit in compliance with ISO 19011</li>
</ul>
<p> </p>
<p>Course Agenda</p>
<p> </p>
<ul>
<li><span><strong>Day 1</strong>:</span> Introduction to Medical Devices Quality Management Systems (MDQMS) and ISO 13485</li>
<li><span><strong>Day 2</strong>:</span> Audit principles, preparation and launching of an audit</li>
<li><span><strong>Day 3</strong>:</span> On-site audit activities </li>
<li><span><strong>Day 4</strong>: </span>Closing the audit and final exam.</li>
</ul>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Assessment</h2>
                        <div>
                            <p> </p>
<p> </p>
<p>Delegates sit a combined exam, consisting of in-course quizzes and exercises, as well as a final essay style exam, consisting of 12 questions, on Day 4 of the course. The overall passing score is 70%, to be achieved within the 150 minute time allowance.</p>
<p>Exam results are provided within 24 hours, with both a Certificate and a digital badge provided as proof of success.</p>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Prerequisites</h2>
                        <div>
                            <p> </p>
<p><span>An understanding of ISO 13485 requirements and knowledge of audit principles.</span></p>
                        </div>
                    </div>
                    <div>
                        <h2>What's Included?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Certification fees are included on the exam price</li>
<li>Training material containing over 500 pages of information and practical examples will be distributed</li>
<li>An attestation of course completion worth 32 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Who Should Attend?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Auditors seeking to perform Medical Devices Quality Management System (MDQMS) certification audits </li>
<li>Managers or consultants seeking to understand the Medical Devices Quality Management System audit requirements</li>
<li>Individuals responsible for maintaining conformance with Medical Devices Quality Management System requirements</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Accreditation</h2>
                        <div>
                            <p><img src="https://www.the-training-centre.com/content/img/National%20Accreditation%20Service%20(3).jpg" height="201" width="258" /></p>
                        </div>
                    </div>
                    <div>
                        <h2>Provided by</h2>
                        <div>
                            <p> </p>
<p>This course is Accredited by <a title="NACS" href="http://www.nacs.ee" target="_blank">NACS</a> and Administered by the <a title="IECB" href="https://www.iecb.org" target="_blank">IECB</a></p>
                        </div>
                    </div>

ISO 13485 Lead Auditor

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					<div><p>The Essentials of European Medical Device Regulations course provides a comprehensive overview of the EU MDR, covering everything from classification and reporting to quality systems. You'll learn from experienced professionals and gain the knowledge and skills to successfully ensure your devices comply with the latest regulations and bring them to market.</p><p>In the first section, you will explore the European Medical Device Regulations (EU MDR). Picture yourself gaining a bird's-eye view of the regulatory framework governing European medical devices. As you delve into the essential components of EU MDR in Section 02, envision yourself gaining a profound understanding of device classification, conformity assessment procedures, and the intricacies of clinical evaluations. It's a voyage of discovery that lays the foundation for your expertise.</p><p>Now, picture yourself in Section 03, where you dive into the depths of reporting requirements and identification. You'll acquire the knowledge and confidence to navigate adverse event reporting and product seamlessly recalls. Finally, in Section 04, envision yourself immersed in the world of quality systems within medical device regulation. Gain the skills to ensure product safety and efficacy while adhering to the highest industry standards.</p><p>By completing this course, you'll emerge as a knowledgeable and adept professional ready to conquer the challenges of European Medical Device Regulations. Whether you're a seasoned industry expert seeking to sharpen your skills or a newcomer eager to embark on a rewarding healthcare career, this course is your gateway to success. Join us on this captivating journey and become a master of European medical device compliance.</p><p>Are you ready to embark on a transformative journey through the intricacies of European Medical Device Regulations? Enroll today and unlock the secrets to compliance, quality, and success in the healthcare industry.</p></div>
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			<h2><b> Learning outcome</b></h2>		</div>
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				<div>
					<ul>
							<li>
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													</span>
										<span>Master the fundamentals of European Medical Device Regulations.</span>
									</li>
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										<span>Understand the key components of EU MDR, including classification and conformity assessment.</span>
									</li>
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													</span>
										<span>Learn how to navigate reporting requirements and handle identification in compliance with regulations.</span>
									</li>
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													</span>
										<span>Gain proficiency in quality systems integral to medical device regulation.</span>
									</li>
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											<span>
													</span>
										<span>Acquire the skills needed to ensure product safety and efficacy.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					</div>
				</div>
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				<div>
					
			</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Why should I take this course?</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Gain a comprehensive understanding of the EU MDR and its requirements</span>
									</li>
								<li>
											<span>
													</span>
										<span>Learn from experienced professionals who have helped companies comply with the EU MDR</span>
									</li>
								<li>
											<span>
													</span>
										<span>Get the knowledge and skills you need to ensure your devices comply with the latest regulations and bring them to market successfully</span>
									</li>
								<li>
											<span>
													</span>
										<span>Stay ahead of the curve and avoid costly mistakes</span>
									</li>
								<li>
											<span>
													</span>
										<span>Protect the safety and well-being of your patients</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Career Path</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Regulatory Affairs Specialist</span>
									</li>
								<li>
											<span>
													</span>
										<span>Quality Assurance Manager</span>
									</li>
								<li>
											<span>
													</span>
										<span>Medical Device Consultant</span>
									</li>
								<li>
											<span>
													</span>
										<span>Clinical Research Associate</span>
									</li>
								<li>
											<span>
													</span>
										<span>Compliance Analyst</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Requirements</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Basic knowledge of medical devices and healthcare regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to a computer with internet connectivity.</span>
									</li>
								<li>
											<span>
													</span>
										<span>A desire to excel in the field of medical device regulation.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section><div>
                            <div>
                                <h2>Course Curriculum</h2>
                            </div>
                            			<div>
				

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4"><strong>Section 01: Overview to European Regulations on Medical Devices</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Overview to European Regulations on Medical Devices</td><td><span>🕐 00:33:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 02: Essential Components of EU MDR</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Essential Components of EU MDR</td><td><span>🕐 00:29:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 03: Reporting Requirements and Identification</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Reporting Requirements and Identification</td><td><span>🕐 00:16:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 04: Quality System in Medical Device Regulation</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Quality System in Medical Device Regulation</td><td><span>🕐 00:25:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
		                        </div>

Skill Up

Medical Device Development

Master the European Medical Device Regulations (EU MDR) with this comprehensive course. Gain the knowledge and skills you need to comply with the EU MDR and successfully bring your medical devices to market.

Essentials of European Medical Device Regulations

<p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" id="isPasted" fr-original-style=" color: rgb(51, 51, 51);">Part 11 of Title 21 of the US Code of Federal Regulations (21CFR11) sets out requirements that computer systems must meet to satisfy the Food and Drug Administration (FDA) that electronic records and electronic signatures provided by those systems are trustworthy and reliable to the same extent as paper counterparts. The regulation sets out controls and procedures which need to be established and followed for relevant computer systems in FDA-regulated environments. An FDA-regulated environment is a &lsquo;GxP&rsquo; environment operated by an organisation involved in activities leading to the marketing of drugs or medical devices in the USA; examples are drug manufacturing sites, medical device manufacturing sites, analytical laboratories, clinical investigational sites, and nonclinical study laboratories.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">21CFR11 applies to records that are required to be submitted to the FDA, or that are subject to FDA inspection, and that are in electronic form &ndash; that is, as computer files. It applies to all computer systems used to create, modify, maintain, archive, retrieve, or transmit such records &ndash; from a humble spreadsheet program to a complex information management system.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">Companies that market or intend to apply for approval to market drugs or medical devices in the USA must comply with 21CFR11, whether or not they are based in the USA. Suppliers to such companies of materials, equipment, or data that are subject to FDA regulation must also comply.</p>

21CFR11 applies to records that are required to be submitted to the FDA, or that are subject to FDA inspection, and that are in electronic form – that is, as computer files. It applies to all computer systems used to create, modify, maintain, archive, retrieve, or transmit such records – from a humble spreadsheet program to a complex information management system.

ICT01: Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures

<p>Learn the recent EU medical device regulations and alterations and turn yourself into an asset for the health &amp; care job sector. The starting salary of a medical device consultant is at least £35k annually. So, why wait? Just take the course.</p><p>The Medical Device Regulations (EU) course will help you understand the basic requirements and ideas of the European Medical Devices Regulation. This course will walk you through the important elements of EU MDR, including regulatory developments in the European market, the structure of the regulation, and the partners affected by it. It contains critical information on reporting requirements and identification, as well as an overview of the UK Good Manufacturing Practice Guides.</p><p>Therefore, enrol in our Medical Device Regulations (EU) course to enlarge your knowledge and grab the opportunities that are waiting for you in the near future.</p><p><strong>At the end of the course, learners will be able to:</strong></p><ul><li>Learn more about the EU Medical Devices Regulations and their potential applications</li><li>Discover the most recent alterations to the European market's regulations</li><li>Recognise what EU MDR actually implies in practice</li><li>Possess a thorough understanding of identification and reporting requirements</li><li>Learn in-depth information on how the new rules affect producers, importers, distributors, and EU representatives of medical devices</li><li>Recognise the full procedure for CE marking in accordance with the Medical Devices Regulation (MDR)</li></ul><p><strong>Expert Support</strong></p><p>Dedicated tutor support and 24/7 customer support are available to all students with this premium quality course.</p><p><strong>Key Benefits</strong></p><ul><li>Learning materials of the Design course contain engaging voiceover and visual elements for your comfort.</li><li>Get 24/7 access to all content for a full year.</li><li>Each of our students gets full tutor support on weekdays (Monday to Friday)</li></ul><p><strong>Please note</strong>: This course only gives you the theoretical knowledge that you need to excel in this field. This Essentials of European Medical Device Regulations course doesn't entitle you to practise as a professional in this specific field.</p><p><strong>COURSE CURRICULUM</strong></p><p><strong>Essentials of European Medical Device Regulations</strong></p><ul><li>Module 1: Overview to European Regulations on Medical Devices</li><li>Module 2: Essential Components of EU MDR</li><li>Module 3: Reporting Requirements and Identification</li><li>Module 4: Quality System in Medical Device Regulation</li></ul><p><strong>Meet the Accreditation</strong></p><p><strong>The CPD Certification Service (CPD UK</strong>) assures the <strong>Essentials of European Medical Device Regulations</strong> course training and learning activities are relevant, reliable, and upto date.</p><p><strong>Course Assessment </strong></p><p>To simplify the procedure of evaluation and accreditation for learners, we provide an automated assessment system. Upon completion of an online module, you will immediately be given access to a specifically crafted MCQ test. The results will be evaluated instantly, and the score will be displayed for your perusal. For each test, the pass mark will be set to 60%.</p><p>When all tests have been successfully passed, you will be able to order a certificate endorsed by the Quality Licence Scheme.</p><p><strong>Exam &amp; Retakes:</strong></p><p>It is to inform our learners that the initial exam for this online course is provided at no additional cost. In the event of needing a retake, a nominal fee of £9.99 will be applicable.</p><p><strong>Certification</strong></p><p>Upon successful completion of the assessment procedure, learners can obtain their certification by placing an order and remitting a fee of £9 for PDF Certificate and £15 for the Hardcopy Certificate within the UK ( An additional £10 postal charge will be applicable for international delivery).</p><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        10 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by The CPD Certification Service
                                        </div>
                                </div>
                            </div>
                        </div><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <ul><li>Senior Regulatory Affairs Specialist</li><li>Sales Representative CP</li><li>Medical Writer</li><li>Quality System Engineer</li></ul>
                        </div><h2>
        
        <div>Requirements</div>
    </h2>

                        <div id="requirements">
                            <p>This Medical Device Regulations (EU) course is open to all, with no formal entry requirements.</p>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <ul><li>Medical Secretary (£17,500 to £24,000) per annum</li><li>Medical illustrator (£25,654 to £39,026) per annum</li><li>Regulatory Medical Device Engineer (£50,000 to £60,000) per annum</li><li>Regulatory Medical Device Consultant (£50,000 to £60,000) per annum</li><li>Midwife - Medical Device Trainer (£35,000 to £45,000) per annum</li></ul>
                        </div>

Medical Device Regulations (EU) Course

<div id="course-pricing" fr-original-style="" style="box-sizing: border-box;">
          </div><p id="isPasted" fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Explore the intricacies of European Medical Device Regulations (EU MDR) with our comprehensive course.&nbsp;</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Gain a solid understanding of the European regulations governing medical devices, including the essential components of EU MDR. Learn about reporting requirements, identification processes, and the quality system involved in regulating medical devices.</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Throughout the course, you&#39;ll grasp the significance of adhering to regulatory standards and guidelines for medical devices. With expert guidance and accessible online materials, this course provides a great learning experience for individuals from any academic background.&nbsp;</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Upon completion, receive a CPD certificate to validate your knowledge and enhance your career prospects in regulatory affairs, quality assurance, compliance, and more.</span></p><h2 dir="ltr" id="isPasted" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Learning Outcome of EU Medical Device Regulations</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Learn the overview of European regulations governing medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Gain insight into the essential components of EU Medical Device Regulations (MDR).</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Understand the reporting requirements and identification processes related to medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Acquire knowledge about the quality system involved in regulating medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Learn about compliance with EU MDR standards and guidelines.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Understand the importance of adhering to regulatory requirements for medical devices.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Key Features of the Course</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">A CPD certificate that is recognised worldwide.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">A great online learning experience.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Interesting and unique online materials and activities.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Expert guidance and support from the field leaders.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Access to the study resources anytime you want.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Friendly and helpful customer service and admin support by email, phone, and chat from Monday through Friday.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Get a year-long access to the course.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Requirements</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">No prerequisites; suitable for individuals from any academic background.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Accessible course materials from any internet-enabled device.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">CPD Certificate from Course Gate</span></h2><p dir="ltr" fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">At the successful completion of the course, you can obtain your CPD certificate from us. You can order the PDF certificate for &pound;9 and the hard copy for &pound;15. Also, you can order both PDF and hardcopy certificates for &pound;22.</span></p><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Career path</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Regulatory Affairs Specialist</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Quality Assurance Manager</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Compliance Officer</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Product Safety Manager</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Clinical Affairs Specialist</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Medical Device Consultant</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Course Curriculum</span><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);"><br fr-original-style="" style="box-sizing: border-box;"></span></h2><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><section fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></section><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 01: Overview to European Regulations on Medical Devices</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 02: Essential Components of EU MDR</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 03: Reporting Requirements and Identification</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 04: Quality System in Medical Device Regulation</li></ul></div>

Course Gate

Explore the essentials of European Medical Device Regulations (EU MDR) with our comprehensive course. Gain insights into regulatory requirements, quality systems, and reporting protocols to ensure compliance in the healthcare industry.

Essentials EU Medical Device Regulations

<p>Do you want to improve your career prospects in Health and Care? One Education brings a range of high-quality Health and Care courses that are ideal for you, whether you're a beginner or aspire for higher roles in research, leadership, and education.</p><p>This <strong>Essentials of European Medical Device Regulations - CPD Certified Course </strong>is excellent for improving your knowledge, skill set and competencies in relevant areas of Health and Care.</p><p><strong>Learning Outcomes of the </strong><strong>Essentials of European Medical Device Regulations - CPD Certified</strong><strong> Training:</strong></p><ul><li>Deepen your understanding of the EU Medical Devices Regulations and how it can be applied</li><li>Learn about recent regulatory changes in the European market</li><li>Understand what EU MDR means in practice</li><li>Have an excellent understanding of reporting requirements and identification</li><li>Gain in-depth knowledge of how the new regulations affect medical device manufacturers, importers, distributors and EU Representatives</li><li>Understand the complete process for CE marking under the Medical Devices Regulation (MDR)</li></ul><p>The course is developed after thorough research and expertise from seasoned professionals. Having prior learning is extremely helpful if you aim to enter the Health and Care sector as a beginner.</p><p>This will be delivered exclusively through our online platform, where you completely control your learning experience. You can go through the modules and study materials at your own pace without any restrictions. And you'll receive a recognised certificate as proof of your newly acquired or improved knowledge and skills.</p><p><strong>Why choose CPD Certification Service Accredited (CPD UK) course?</strong></p><ul><li>World's leading and largest independent CPD accreditation institution</li><li>Pioneering CPD quality standards since 1996</li><li>Over 20 thousand registered CPD Providers and Courses</li><li>With 25 years experience providing industry-leading CPD certification service and support</li></ul><p>Take a step towards reaching your true potential by enrolling in this <strong> Essentials of European Medical Device Regulations - CPD Certified Training</strong>!</p><p>Understand the essential requirements and concepts of the European Medical Devices Regulation, with the Essentials of European Medical Device Regulations course. This course covers the essential components of EU MDR, taking you through regulatory changes in the European market, the structure of the regulation and the partners affected by it. It includes important information on reporting requirements and identification, as we as an overview of the UK Guides to Good Manufacturing Practice.</p><p>Please note: This course only gives you the theoretical knowledge that you need to excel in this field. This Essentials of European Medical Device Regulations doesn't entitle you to practise as a professional in this specific field.</p><p><strong>Course Curriculum:</strong></p><ul><li>Module 1: Overview to European Regulations on Medical Devices</li><li>Module 2: Essential Components of EU MDR</li><li>Module 3: Reporting Requirements and Identification</li><li>Module 4: Quality System in Medical Device Regulation</li></ul><p><strong>Course Assessment</strong></p><p>You will immediately be given access to a specifically crafted MCQ test upon completing an online module. For each test, the pass mark will be set to 60%.</p><p><strong>Exam &amp; Retakes:</strong><br />It is to inform our learners that the initial exam for this online course is provided at no additional cost. In the event of needing a retake, a nominal fee of £9.99 will be applicable.</p><p><strong>Certification</strong><br />Upon successful completion of the assessment procedure, learners can obtain their certification by placing an order and remitting a fee of £9 for PDF Certificate and £15 for the Hardcopy Certificate within the UK ( An additional £10 postal charge will be applicable for international delivery).</p><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        10 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by The CPD Certification Service
                                        </div>
                                </div>
                            </div>
                        </div><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <p>The <strong>Essentials of European Medical Device Regulations - CPD Certified</strong> training is ideal for highly motivated individuals or teams who want to enhance their professional skills and efficiently skilled employees.</p>
                        </div><h2>
        
        <div>Requirements</div>
    </h2>

                        <div id="requirements">
                            <p>There are no formal entry requirements for the course, with enrollment open to anyone!</p>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <p>Learn the essential skills and knowledge you need to excel in your professional life with the help &amp; guidance from our <strong>Essentials of European Medical Device Regulations - CPD Certified</strong> training.</p>
                        </div><h2>
        
        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>Certificate of completion</h4>
        <p>
            Digital certificate -
            £9
        </p>
        <h4>Certificate of completion</h4>
        <p>
            Hard copy certificate -
            £15
        </p>
            <div> <p><strong>CPD Certification Service Accredited Certification</strong></p><ul><li>Hardcopy Certificate (within the UK): £15</li><li>Hardcopy Certificate (international): £15 + £10 (postal charge) = £25</li></ul> </div>

                        </div>

Essentials of European Medical Device Regulations - CPD Certified Course

<p>Delve into the intricacies of European medical device regulatory frameworks with our comprehensive course, '<strong>Essentials of European Medical Device Regulations</strong>.' This meticulously structured program provides an in-depth exploration of the critical components and legislative requirements necessary for navigating the complex landscape of medical device regulations in Europe. The first module introduces the foundational aspects of the European regulations, setting the stage for a deeper understanding of the legal and procedural elements that govern this sector. As the course progresses, participants will gain a thorough grasp of the Essential Components of EU MDR (Module 2), the pivotal aspects of Reporting Requirements and Identification (Module 3), and the integral role of Quality Systems in medical device regulation (Module 4). This course is meticulously designed to cater to the needs of professionals seeking a robust understanding of the regulatory environment, ensuring they are well-equipped to adhere to and implement these critical regulations.</p>
<p><strong>Learning Outcomes</strong></p>
<ul>
<li>Acquire a solid foundation in the basic principles and framework of European regulations on medical devices.</li>
<li>Understand the key elements of the EU Medical Device Regulation (MDR) and their application in the industry.</li>
<li>Gain insights into the specific requirements for reporting and identification within the European regulatory context.</li>
<li>Learn about the implementation and management of quality systems in compliance with medical device regulations.</li>
<li>Develop the ability to interpret and apply regulatory guidelines in professional settings, enhancing compliance and operational efficiency.</li>
</ul>
<h3><b>Why choose this Essentials of European Medical Device Regulations<span> course</span>?</b></h3>
<ol>
<li>Unlimited access to the course for a lifetime.</li>
<li>Opportunity to earn a certificate accredited by the <b>CPD Quality Standards</b> and <b>CIQ </b>after completing this course.</li>
<li>Structured lesson planning in line with industry standards.</li>
<li>Immerse yourself in innovative and captivating course materials and activities.</li>
<li>Assessments designed to evaluate advanced cognitive abilities and skill proficiency.</li>
<li>Flexibility to complete the Course at your own pace, on your own schedule.</li>
<li>Receive full tutor support throughout the week, from Monday to Friday, to enhance your learning experience.</li>
<li>Unlock career resources for CV improvement, interview readiness, and job success.</li>
</ol>
<h3><b>Who is this Essentials of European Medical Device Regulations<span> </span></b><b><span>course </span></b><b>for?</b></h3>
<ul>
<li>Professionals in the medical device industry seeking to deepen their understanding of EU regulations.</li>
<li>Regulatory affairs specialists aiming to stay updated with the latest European legislative changes.</li>
<li>Quality assurance personnel in the healthcare sector requiring knowledge of regulatory compliance.</li>
<li>Medical device manufacturers and distributors needing to align their products with EU standards.</li>
<li>Healthcare consultants and advisors focusing on European medical device regulatory frameworks.</li>
</ul>
<h3><b>Career path</b></h3>
<ul>
<li><strong>Regulatory Affairs Manager</strong>: £40,000 - £60,000</li>
<li><strong>Quality Assurance Specialist</strong>: £35,000 - £50,000</li>
<li><strong>Compliance Officer</strong>: £30,000 - £45,000</li>
<li><strong>Product Development Engineer</strong>: £33,000 - £55,000</li>
<li><strong>Healthcare Consultant</strong>: £45,000 - £70,000</li>
<li><strong>Medical Device Auditor</strong>: £37,000 - £53,000</li>
</ul>
<h3><b>Prerequisites</b></h3>
<p><span>This </span><b>Essentials of European Medical Device Regulations</b><span> does not require you to have any prior qualifications or experience. You can just enrol and start learning. This </span><span>course</span><span> was made by professionals and it is compatible with all PC's, Mac's, tablets and smartphones. You will be able to access the course from anywhere at any time as long as you have a good enough internet connection.</span></p>
<h3><b>Certification</b></h3>
<p><span>After studying the course materials, there will be a written assignment test which you can take at the end of the course. After successfully passing the test you will be able to claim the pdf certificate for £4.99 Original Hard Copy certificates need to be ordered at an additional cost of £8.</span></p><div>
				<h3>
	<span>Course Curriculum</span>
</h3>

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4">Module 1: Overview to European Regulations on Medical Devices</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Overview to European Regulations on Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:43:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 2: Essential Components of EU MDR</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Essential Components of EU MDR</td>
					<td> </td>
					<td><span><i></i> 00:40:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 3: Reporting Requirements and Identification</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Reporting Requirements and Identification</td>
					<td> </td>
					<td><span><i></i> 00:27:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 4: Quality System in Medical Device Regulation</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Quality System in Medical Device Regulation</td>
					<td> </td>
					<td><span><i></i> 00:36:00</span></td>
				</tr>
				</tbody></table></div>

			</div>

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